A magnetically separable palladium catalyst containing a bulky N-heterocyclic carbene ligand for the Suzuki–Miyaura reaction-Reference-Cited by-同舟云学术

A magnetically separable palladium catalyst containing a bulky N-heterocyclic carbene ligand for the Suzuki–Miyaura reaction

Published:2015 Issue:1 Volume:17 Page:413-420
ISSN:1463-9262
Container-title:Green Chemistry
language:en
Short-container-title:Green Chem.

Author:

Wang Z.¹²³⁴,Yu Y.¹²³⁴,Zhang Y. X.⁵²³⁴,Li S. Z.¹²³⁴,Qian H.¹²³⁴,Lin Z. Y.⁶⁷²³⁴

Affiliation:

1. College of Material Science and Engineering

2. Huaqiao University

3. XiaMen 361021

4. China

5. College of Communication Science and Engineering

6. Engineering Research Center of Environment-Friendly Functional Materials

7. Ministry of Education

Abstract

Bulky NHC ligands were employed for preparing magnetic palladium catalysts, which showed excellent activity, stability and reusability towards the Suzuki–Miyaura reaction.

Publisher

Royal Society of Chemistry (RSC)

Subject

Pollution,Environmental Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2015/GC/C4GC00574K

Reference58 articles.

1. General Catalysts for the Suzuki-Miyaura and Sonogashira Coupling Reactions of Aryl Chlorides and for the Coupling of Challenging Substrate Combinations in Water

2. Alkyl−Alkyl Suzuki Cross-Couplings of Unactivated Secondary Alkyl Halides at Room Temperature

3. Degrading perchloroethene at ambient conditions using Pd and Pd-on-Au reduction catalysts

4. A General and Efficient Method for the Suzuki–Miyaura Coupling of 2-Pyridyl Nucleophiles

5. The Art of Meeting Palladium Specifications in Active Pharmaceutical Ingredients Produced by Pd-Catalyzed Reactions

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